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Completed

NCT Number: NCT04119440

Safety and Immunogenicity of the Candidate Vaccine MVA-MERS-S_DF-1 Against MERS

The study will be a two center, randomized, double blind, placebo controlled study of the MVA MERS S_DF-1 candidate delivered by i.m. injection. To evaluate the MERS-S-specific antibody responses and safety profile induced by the two dosage levels of MVA-MERS-S_DF-1 the data will be compared to a placebo control group.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

University Medical Center Hamburg-Eppendorf, Hamburg, Germany

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About this study

This will be a Phase Ib, two-center study in approximately 160 healthy adults aged 18-55 years

The study is separated in two parts:

Part A:

The study starts with a single center open-label run-in phase of two dose levels (cohort 1 "low dose": 2x10^7 PFU, cohort 2 "high dose": 2x10^8 PFU) in 10 healthy subjects. 5 subjects will be allocated to each dose cohort and will receive immunization on day 0 and day 28.

Part B:

Two-center, randomized, double-blind, placebo-controlled, dose-finding study. This part is a double-blinded trial in approximately 150 healthy subjects. Subjects will be allocated to two different dose cohorts and a placebo cohort; each receiving three vaccine injections.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent form.
  • Healthy male and female subjects aged 18-55 years.
  • No clinically significant acute health problems as determined from medical history and physical examination at screening visit.
  • Body mass index 18.5 - 30.0 kg/m2 and weight > 50 kg at screening.
  • Non-pregnant, non-lactating female with negative pregnancy test.
  • Males and females who agree to comply with the applicable contraceptive requirements of the protocol.

Exclusion criteria

  • Receipt of any vaccine from 2 weeks prior to each trial vac-cination (4 weeks for live vaccines) to 3 weeks after each trial vaccination.
  • Receipt of vaccination against MERS or MVA immunizations.in the medical history.
  • Known allergy to the components of the MVA-MERS-S_DF-1 vaccine product.
  • Evidence in the subject's medical history or in the medical examination that might influence either the safety of the subject or the absorption, distribution, metabolism or excretion of the investigational product.
  • Any confirmed or suspected immunosuppressive or immuno-deficient condition, cytotoxic therapy in the previous 5 years, and/or diabetes.
  • Any chronic or active neurologic disorder, including seizures and epilepsy, excluding a single febrile seizure as a child.

Treatment and study plan

MVA-MERS-S_DF1 - Low Dose

Biological

Administrations of the low dose via the intramuscular route

MVA-MERS-S_DF1 - High Dose

Biological

Administrations of the high dose via the intramuscular route

Placebo

Other

Administrations of placebo via the intramuscular route

Primary outcomes

  1. Frequency of adverse events associated with MVA-MERS-S_DF-1.

    Time frame: day 1, 14, 29, 42, 56, 84, 168, 336, 364

    Safety and reactogenicity will be assesssed by observation, questionaire and diary. Changes from baseline for safety laboratory measures will be monitored. Occurence of SAE will be collected throughout the entire study duration.

  2. Frequency and severity of local injection site reactogenicity signs and symptoms

    Time frame: day 1, 14, 29, 42, 84, 336

Secondary outcomes

  1. Immunogenicity

    Time frame: day 0, 14, 28, 42, 56, 70, 84, 168, 336, 364 (dependent on vaccination scheme)

    Magnitude of MERS-S-specific antibody re-sponses (ELISA and neutralization assays) monitored in a centralized approved laboratory

Sponsors and collaborators

Lead sponsor

Universitätsklinikum Hamburg-Eppendorf

Other

Collaborators

  • CR2O
  • Coalition for Epidemic Preparedness Innovations
  • Erasmus Medical Center
  • German Center for Infection Research
  • IDT Biologika Dessau.Rossau
  • Monipol Deutschland GmbH

Registry information

Official study title

A Two-center, Randomized, Double-blind, Placebo-controlled, Phase Ib Study to Assess the Safety, Tolerability and Immunogenicity of Two Ascending Doses of the Candidate Vaccine MVA-MERS-S_DF-1 in Healthy Study Subjects

Acronym: MVA-MERS-S

Important dates

Study start
2021
Primary completion
2022
Study completion
2024
First posted
Oct 8, 2019
Registry last updated
Apr 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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